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CAS 171364-85-5

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QUINOLINE-3-BORONIC ACID PINACOLATE

Description:
Quinoline-3-boronic acid pinacolate is an organoboron compound characterized by the presence of a quinoline moiety and a boronic acid functional group. This compound typically exhibits properties associated with both boronic acids and quinoline derivatives, such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, particularly in Suzuki-Miyaura coupling. The boronic acid group allows for the formation of stable complexes with diols and can participate in various organic transformations, making it valuable in synthetic chemistry. The pinacolate ester formation provides enhanced stability and solubility, facilitating its use in diverse applications, including medicinal chemistry and materials science. Additionally, quinoline derivatives are known for their biological activity, which may extend to this compound, suggesting potential applications in drug development. Overall, quinoline-3-boronic acid pinacolate is a versatile compound with significant utility in organic synthesis and potential pharmacological applications.
Formula:C15H18BNO2
InChI:InChI=1/C15H18BNO2/c1-14(2)15(3,4)19-16(18-14)12-9-11-7-5-6-8-13(11)17-10-12/h5-10H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cc3ccccc3nc2)O1
Synonyms:
  • Akos Brn-1143
  • 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Quinoline
  • 3-Quinolineboronic Acid Pinacol Ester
  • Quinoline-3-Boronic Acid Pinacol Ester
  • 3-Quinolineboronic acid pinacol ester 95%
  • 4,4,5,5-Tetramethyl-2-(3-quinolyl)-1,3,2-dioxaborolane
  • 3-hydroxy-2,3-diMethylbutan-2-yl hydrogen quinolin-3-ylboronate
  • quinoline-boronic acid pinacol ester
  • QUINOLINE-3-BORONIC ACID PINACOLATE
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolone
  • See more synonyms
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